Principal Toxicologist

We are seeking a highly motivated Research Scientist to join our Health and Environmental Sciences (HES) team at PI Industries Ltd. The ideal candidate will play a crucial role in planning, designing, and executing in vitro experiments to evaluate new molecules' safety and efficacy.

Key Responsibilities:

• Experiment Planning and Execution: Design and conduct in vitro experiments, including but not limited to AMES, Steroidogenesis, Chromosomal Aberrations, Micronucleus, Cell Gene Mutation, and ERT assays.
• Ensure experiments are conducted in accordance with regulatory standards and organizational protocols.
• Cell Line Maintenance: Maintain and culture various cell lines and bacterial cells, ensuring optimal conditions for experimental use.
• Laboratory Operations: Operate laboratory equipment and instruments, applying relevant technologies in the preparation of media, reagents, and solutions required for experiments.
• Validate new study designs as necessary to enhance experimental outcomes.
• Data Collection and Analysis: Collect, analyze, and interpret experimental data, preparing technical summaries for departmental review.
• Document and maintain electronic technical data generated within the department.
• Standard Operating Procedures (SOPs): Write and review departmental SOPs to ensure consistency and compliance with best practices.
• Scientific Communication: Deliver scientific and technical presentations within the department, sharing findings and insights from research activities.
• Attain required knowledge through continuous learning, attending seminars, workshops, and conferences to stay updated on advancements in the field of in vitro toxicology.
• Explore and implement computational tools and in silico models related to genotoxicity research.
• Safety Compliance: Adhere to organizational policies concerning the safe handling and conduct of all laboratory experiments.

Qualifications: Ph.D. (Preferable) or Master's degree in Toxicology, Biochemistry, or Molecular Biology.

Experience: At least 5 years of experience in conducting in vitro toxicological assays and experience with cell culture techniques from a OECD GLP Certified laboratory or CRO or reputed institute.

Skills: Proficiency in data analysis software and technical writing.

Personal Qualities: Excellent organizational skills and ability to manage multiple projects simultaneously. Strong communication and interpersonal skills, with the ability to work collaboratively in a team environment.